催化作用
路易斯酸
氧化还原
布朗斯特德-洛瑞酸碱理论
穆斯堡尔谱学
多孔性
化学
退火(玻璃)
无机化学
化学工程
材料科学
结晶学
有机化学
冶金
工程类
作者
Amarajothi Dhakshinamoorthy,Mercedes Ãlvaro,Patricia Horcajada,Emma K. Gibson,M. Vishnuvarthan,Alexandré Vimont,Jean‐Marc Grenèche,Christian Serre,Marco Daturi,Hermenegildo Garcı́a
摘要
Two porous iron trimesates, namely, commercial Basolite F300 (Fe(BTC); BTC = 1,3,5-benzenetricarboxylate) with unknown structure and synthetic MIL-100(Fe) (MIL stands for Material of Institut Lavoisier) of well-defined crystalline structure, have been compared as heterogeneous catalysts for four different reactions. It was found that while for catalytic processes requiring strong Lewis acid sites, Fe(BTC) performs better, MIL-100(Fe) is the preferred catalyst for oxidation reactions. These catalytic results have been rationalized by a combined in situ infrared and 57Fe Mössbauer spectroscopic characterization. It is proposed that the presence of extra Brønsted acid sites on the Fe(BTC) and the easier redox behavior of the MIL-100(Fe) could explain these comparative catalytic performances. The results illustrate the importance of structural defects (presence of weak Brønsted acid sites) and structural stability (MIL-100(Fe) is stable upon annealing at 280 °C despite Fe3+-to-Fe2+ reduction) on the catalytic activity of these two solids, depending on the reaction type.
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